POMT2 and POMT1

Number of citations of the paper that reports this interaction (PubMedID 14699049)
43

Data Source:
HPRD (in vitro, in vivo)

		POMT2	POMT1
Description		protein O-mannosyltransferase 2	protein O-mannosyltransferase 1
Image		No pdb structure	No pdb structure
GO Annotations	Cellular Component	Nucleoplasm Nucleolus Endoplasmic Reticulum Endoplasmic Reticulum Membrane Cytosol Membrane	Acrosomal Vesicle Endoplasmic Reticulum Endoplasmic Reticulum Membrane Membrane Sarcoplasmic Reticulum Dolichyl-phosphate-mannose-protein Mannosyltransferase Complex
	Molecular Function	Mannosyltransferase Activity Dolichyl-phosphate-mannose-protein Mannosyltransferase Activity Transferase Activity Glycosyltransferase Activity Metal Ion Binding	Mannosyltransferase Activity Dolichyl-phosphate-mannose-protein Mannosyltransferase Activity Protein Binding Transferase Activity Glycosyltransferase Activity Metal Ion Binding
	Biological Process	Protein Glycosylation Protein O-linked Glycosylation Dentate Gyrus Development Protein O-linked Glycosylation Via Mannose Basement Membrane Organization Reactive Gliosis	Protein Glycosylation Protein O-linked Glycosylation Extracellular Matrix Organization Protein O-linked Glycosylation Via Mannose
Pathways		Defective POMT2 causes MDDGA2, MDDGB2 and MDDGC2 Defective POMT1 causes MDDGA1, MDDGB1 and MDDGC1 DAG1 core M2 glycosylations DAG1 core M3 glycosylations DAG1 core M1 glycosylations Regulation of CDH1 posttranslational processing and trafficking to plasma membrane	Defective POMT2 causes MDDGA2, MDDGB2 and MDDGC2 Defective POMT1 causes MDDGA1, MDDGB1 and MDDGC1 DAG1 core M2 glycosylations DAG1 core M3 glycosylations DAG1 core M1 glycosylations Regulation of CDH1 posttranslational processing and trafficking to plasma membrane
Drugs
Diseases		Dystroglycanopathy; Walker-Warburg syndrome (WWS); Muscle-eye-brain disease (MEB); Fukuyama congenital muscular dystrophy (FCMD); Congenital muscular dystrophy with muscle hypertrophy (MDC1C); Congenital muscular dystrophy with severe intellectual impairment and abnormal glycosylation (MDC1D) Limb-girdle muscular dystrophy (LGMD) Congenital muscular dystrophies (CMD/MDC), including: Merosin-deficient CMD (MDC1A); Ullrich CMD (UCMD); Integrin alpha7-deficient CMD; CMD with joint hyperlaxity (CMDH); CMD with epidermolysis bullosa; Walker-Warburg syndrome (WWS); Muscle-eye-brain disease (MEB); Fukuyama CMD (FCMD); CMD with muscle hypertrophy (MDC1C); CMD with severe intellectual impairment and abnormal glycosylation (MDC1D); Rigid spine syndrome (RSS); LMNA-deficient CMD; CMD with respiratory failure and muscle hypertrophy (MDC1B); Bethlem myopathy	Dystroglycanopathy; Walker-Warburg syndrome (WWS); Muscle-eye-brain disease (MEB); Fukuyama congenital muscular dystrophy (FCMD); Congenital muscular dystrophy with muscle hypertrophy (MDC1C); Congenital muscular dystrophy with severe intellectual impairment and abnormal glycosylation (MDC1D) Limb-girdle muscular dystrophy (LGMD) Congenital muscular dystrophies (CMD/MDC), including: Merosin-deficient CMD (MDC1A); Ullrich CMD (UCMD); Integrin alpha7-deficient CMD; CMD with joint hyperlaxity (CMDH); CMD with epidermolysis bullosa; Walker-Warburg syndrome (WWS); Muscle-eye-brain disease (MEB); Fukuyama CMD (FCMD); CMD with muscle hypertrophy (MDC1C); CMD with severe intellectual impairment and abnormal glycosylation (MDC1D); Rigid spine syndrome (RSS); LMNA-deficient CMD; CMD with respiratory failure and muscle hypertrophy (MDC1B); Bethlem myopathy
GWAS
Interacting Genes		3 interacting genes: GLP1R LINC00839 POMT1	2 interacting genes: MEOX2 POMT2
Entrez ID		29954	10585
HPRD ID		09592	06305
Ensembl ID		ENSG00000009830	ENSG00000130714
Uniprot IDs		Q9UKY4	A0A140VKE0 A0A7I2V2K0 A0A7I2V445 B4DTW4 Q5JT02 Q9Y6A1
PDB IDs
Enriched GO Terms of Interacting Partners?		Glucagon-like Peptide 1 Receptor Activity Dolichyl-phosphate-mannose-protein Mannosyltransferase Complex Response To Psychosocial Stress Glucagon Receptor Activity Dolichyl-phosphate-mannose-protein Mannosyltransferase Activity Post-translational Protein Targeting To Membrane, Translocation Cellular Response To Glucagon Stimulus Protein O-linked Glycosylation Via Mannose Mannosyltransferase Activity Activation Of Adenylate Cyclase Activity Positive Regulation Of Lyase Activity Positive Regulation Of Adenylate Cyclase Activity Response To Glucagon Positive Regulation Of Cyclase Activity Intracellular Protein Transmembrane Transport Positive Regulation Of Blood Pressure Peptide Hormone Binding G Protein-coupled Peptide Receptor Activity Negative Regulation Of Blood Pressure	Cytoplasmic Side Of Nuclear Pore Somite Specification Reactive Gliosis Dolichyl-phosphate-mannose-protein Mannosyltransferase Activity Segment Specification Somite Development Nuclear Export Signal Receptor Activity Protein O-linked Glycosylation Via Mannose Neuroinflammatory Response Mannosyltransferase Activity Structural Constituent Of Nuclear Pore Nuclear Localization Sequence Binding
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